Effects of Masseter Manual Therapy on Temporomandibular Dysfunction: A Pilot Study
Trial Snapshot
- Phase
- Phase 1
- Enrollment
- 45
- Locations
- 2
- Primary Endpoint
- Range of Motion
Study Overview
Brief Summary
Muscles and myofascial dysfunction are more often the mechanism and source of pain in oral fascial disorders (OFD) than the TMJ. Masticatory muscles in patients with TMJ alterations are more hypertonic, less efficient and more prone to fatigue compared to age and sex matched controls. It is our opinion that Active Release Technique can be a reliable assessment and treatment tool in the resolution in cervical-cranio mandibular disorders. Our goal is to improve masticatory function through treatment of trigger points in the masseter.
Detailed Description
Recruit 45 patients with TMD determined by questionnaire. Measure pre and post mandibular active range of motion and VAS pain scale. Treatment will include 4 visits over a two week span measuring before first treatment and after last treatment. There will be 3 treatment groups; active release technique, post isometric relaxation and a no treatment control group. We will analyze data for any change in mandibular range of motion and VAS pain scale.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Difficulty and/or pain when opening mouth
- •Jaw locking
- •Difficulty or pain when chewing or talking
- •TMJ clicking
- •Jaw stiffness, tightness, or fatigue
- •Pain in ear, temple or cheeks
- •Frequent headaches, neckaches, toothaches
- •Change in occlusion
Exclusion Criteria
- •Trauma to head, neck or jaw within last 12 months
- •Recent dental extractions
- •Taking prescription analgesics/muscle relaxants
- •Recent cervical SMT (HVLA)
- •Already under care for condition
- •Sinus infection
Outcomes
Primary Outcomes
Range of Motion
Time Frame: 2 weeks
Secondary Outcomes
- VAS pain scale(2 Weeks)